about
Hypertrophic cardiomyopathy in childhoodA new mutation of the cardiac troponin T gene causing familial hypertrophic cardiomyopathy without left ventricular hypertrophyDisease-causing mutations in cardiac troponin T: identification of a critical tropomyosin-binding regionLong-term follow-up of R403WMYH7 and R92WTNNT2 HCM families: mutations determine left ventricular dimensions but not wall thickness during disease progressionThin filament mutations: developing an integrative approach to a complex disorderA truncated cardiac troponin T molecule in transgenic mice suggests multiple cellular mechanisms for familial hypertrophic cardiomyopathyCardiac troponin T mutations result in allele-specific phenotypes in a mouse model for hypertrophic cardiomyopathyChanges in the chemical and dynamic properties of cardiac troponin T cause discrete cardiomyopathies in transgenic mice.Myofilament Ca2+ sensitization causes susceptibility to cardiac arrhythmia in mice.Temporal and mutation-specific alterations in Ca2+ homeostasis differentially determine the progression of cTnT-related cardiomyopathies in murine models.Pathogenic peptide deviations support a model of adaptive evolution of chordate cardiac performance by troponin mutations.Prognostic predictive value of gene mutations in Japanese patients with hypertrophic cardiomyopathy.Genetic causes of human heart failure.Mechanochemotransduction during cardiomyocyte contraction is mediated by localized nitric oxide signaling.The origins of hypertrophic cardiomyopathy-causing mutations in two South African subpopulations: a unique profile of both independent and founder eventsMendelian-inherited heart disease: a gateway to understanding mechanisms in heart disease Update on work done at the University of StellenboschNovel genotype-phenotype associations demonstrated by high-throughput sequencing in patients with hypertrophic cardiomyopathyCardiac myosin heavy chain isoform exchange alters the phenotype of cTnT-related cardiomyopathies in mouse hearts.Clinical phenotype and outcome of hypertrophic cardiomyopathy associated with thin-filament gene mutations.VIP gene deletion in mice causes cardiomyopathy associated with upregulation of heart failure genes.Research priorities in hypertrophic cardiomyopathy: report of a Working Group of the National Heart, Lung, and Blood Institute.Molecular mechanisms of inherited cardiomyopathies.Genetics and clinical destiny: improving care in hypertrophic cardiomyopathyMolecular diagnosis of myocardial disease.Echocardiographic pitfalls in the diagnosis of hypertrophic cardiomyopathyStructural and functional aspects of the myosin essential light chain in cardiac muscle contraction.The pathology of hypertrophic cardiomyopathy.Delayed hyperenhancement in magnetic resonance imaging of left ventricular hypertrophy caused by aortic stenosis and hypertrophic cardiomyopathy: visualisation of focal fibrosisPhenotype and prognostic correlations of the converter region mutations affecting the β myosin heavy chainMyocardial regulatory proteins and heart failure.Genomics and cardiovascular disease.Impact of Mendelian inheritance in cardiovascular disease.Sudden cardiac death not related to coronary atherosclerosis.Molecular effects of familial hypertrophic cardiomyopathy-related mutations in the TNT1 domain of cTnT.Early results of sarcomeric gene screening from the Egyptian National BA-HCM Program.Genetic basis of hypertrophic cardiomyopathy.Genetic complexity in hypertrophic cardiomyopathy revealed by high-throughput sequencing.Functional analyses of troponin T mutations that cause hypertrophic cardiomyopathy: insights into disease pathogenesis and troponin function.Proteomic analysis of physiological versus pathological cardiac remodeling in animal models expressing mutations in myosin essential light chains.Cardiac troponin T mutation in familial cardiomyopathy with variable remodeling and restrictive physiology.
P2860
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P2860
description
1997 nî lūn-bûn
@nan
1997 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի մարտին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
Sudden death due to troponin T mutations
@ast
Sudden death due to troponin T mutations
@en
Sudden death due to troponin T mutations
@nl
type
label
Sudden death due to troponin T mutations
@ast
Sudden death due to troponin T mutations
@en
Sudden death due to troponin T mutations
@nl
prefLabel
Sudden death due to troponin T mutations
@ast
Sudden death due to troponin T mutations
@en
Sudden death due to troponin T mutations
@nl
P2093
P3181
P1476
Sudden death due to troponin T mutations
@en
P2093
P304
P3181
P356
10.1016/S0735-1097(96)00530-X
P407
P577
1997-03-01T00:00:00Z